Cobalt in PDB 3qyh: Crystal Structure of Co-Type Nitrile Hydratase Beta-H71L From Pseudomonas Putida.
Protein crystallography data
The structure of Crystal Structure of Co-Type Nitrile Hydratase Beta-H71L From Pseudomonas Putida., PDB code: 3qyh
was solved by
H.R.Brodkin,
W.R.P.Novak,
D.Ringe,
G.A.Petsko,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
45.40 /
2.00
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
81.978,
137.657,
85.453,
90.00,
92.45,
90.00
|
R / Rfree (%)
|
16.8 /
20.2
|
Cobalt Binding Sites:
The binding sites of Cobalt atom in the Crystal Structure of Co-Type Nitrile Hydratase Beta-H71L From Pseudomonas Putida.
(pdb code 3qyh). This binding sites where shown within
5.0 Angstroms radius around Cobalt atom.
In total 4 binding sites of Cobalt where determined in the
Crystal Structure of Co-Type Nitrile Hydratase Beta-H71L From Pseudomonas Putida., PDB code: 3qyh:
Jump to Cobalt binding site number:
1;
2;
3;
4;
Cobalt binding site 1 out
of 4 in 3qyh
Go back to
Cobalt Binding Sites List in 3qyh
Cobalt binding site 1 out
of 4 in the Crystal Structure of Co-Type Nitrile Hydratase Beta-H71L From Pseudomonas Putida.
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 1 of Crystal Structure of Co-Type Nitrile Hydratase Beta-H71L From Pseudomonas Putida. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Co212
b:11.0
occ:1.00
|
N
|
A:SER116
|
2.0
|
10.6
|
1.0
|
N
|
A:CSD117
|
2.0
|
12.6
|
1.0
|
SG
|
A:CSD117
|
2.2
|
10.8
|
1.0
|
SG
|
A:CSD115
|
2.2
|
11.0
|
1.0
|
SG
|
A:CYS112
|
2.4
|
10.9
|
1.0
|
C
|
A:SER116
|
2.8
|
9.7
|
1.0
|
CA
|
A:SER116
|
2.9
|
11.7
|
1.0
|
CA
|
A:CSD117
|
3.0
|
13.3
|
1.0
|
OD2
|
A:CSD117
|
3.0
|
27.0
|
1.0
|
CB
|
A:CSD117
|
3.0
|
12.0
|
1.0
|
C
|
A:CSD115
|
3.1
|
12.6
|
1.0
|
OD2
|
A:CSD115
|
3.2
|
12.3
|
1.0
|
OD1
|
A:CSD115
|
3.2
|
13.0
|
1.0
|
CB
|
A:CSD115
|
3.3
|
7.9
|
1.0
|
CB
|
A:CYS112
|
3.4
|
9.8
|
1.0
|
CA
|
A:CSD115
|
3.5
|
11.8
|
1.0
|
OD1
|
A:CSD117
|
3.7
|
26.6
|
1.0
|
OG
|
A:SER116
|
3.7
|
15.4
|
1.0
|
N
|
A:CSD115
|
3.9
|
12.1
|
1.0
|
CB
|
A:SER116
|
3.9
|
9.8
|
1.0
|
O
|
A:SER116
|
4.0
|
10.1
|
1.0
|
O
|
A:CSD115
|
4.2
|
11.5
|
1.0
|
C
|
A:CSD117
|
4.3
|
10.7
|
1.0
|
O
|
A:CSD117
|
4.6
|
8.5
|
1.0
|
CA
|
A:CYS112
|
4.8
|
7.3
|
1.0
|
NH2
|
B:ARG149
|
4.9
|
12.0
|
1.0
|
C
|
A:LEU114
|
4.9
|
10.4
|
1.0
|
|
Cobalt binding site 2 out
of 4 in 3qyh
Go back to
Cobalt Binding Sites List in 3qyh
Cobalt binding site 2 out
of 4 in the Crystal Structure of Co-Type Nitrile Hydratase Beta-H71L From Pseudomonas Putida.
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 2 of Crystal Structure of Co-Type Nitrile Hydratase Beta-H71L From Pseudomonas Putida. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Co212
b:12.2
occ:1.00
|
N
|
C:CSD117
|
2.0
|
12.3
|
1.0
|
N
|
C:SER116
|
2.0
|
12.8
|
1.0
|
SG
|
C:CSD115
|
2.2
|
11.8
|
1.0
|
SG
|
C:CSD117
|
2.2
|
13.1
|
1.0
|
SG
|
C:CYS112
|
2.4
|
13.7
|
1.0
|
C
|
C:SER116
|
2.8
|
18.8
|
1.0
|
CA
|
C:SER116
|
2.9
|
14.9
|
1.0
|
OD2
|
C:CSD117
|
2.9
|
20.9
|
1.0
|
CB
|
C:CSD117
|
3.0
|
12.2
|
1.0
|
CA
|
C:CSD117
|
3.0
|
14.4
|
1.0
|
C
|
C:CSD115
|
3.1
|
15.3
|
1.0
|
OD1
|
C:CSD115
|
3.2
|
15.7
|
1.0
|
OD2
|
C:CSD115
|
3.2
|
13.2
|
1.0
|
CB
|
C:CSD115
|
3.3
|
10.3
|
1.0
|
CB
|
C:CYS112
|
3.4
|
12.6
|
1.0
|
CA
|
C:CSD115
|
3.4
|
11.0
|
1.0
|
OG
|
C:SER116
|
3.6
|
16.3
|
1.0
|
OD1
|
C:CSD117
|
3.7
|
34.6
|
1.0
|
N
|
C:CSD115
|
3.8
|
12.4
|
1.0
|
CB
|
C:SER116
|
3.9
|
14.9
|
1.0
|
O
|
C:SER116
|
4.0
|
15.2
|
1.0
|
O
|
C:CSD115
|
4.2
|
15.4
|
1.0
|
C
|
C:CSD117
|
4.3
|
13.6
|
1.0
|
O
|
C:CSD117
|
4.5
|
14.9
|
1.0
|
CA
|
C:CYS112
|
4.8
|
12.0
|
1.0
|
NH2
|
D:ARG149
|
4.9
|
11.9
|
1.0
|
C
|
C:LEU114
|
4.9
|
11.2
|
1.0
|
O
|
C:CYS112
|
5.0
|
11.9
|
1.0
|
|
Cobalt binding site 3 out
of 4 in 3qyh
Go back to
Cobalt Binding Sites List in 3qyh
Cobalt binding site 3 out
of 4 in the Crystal Structure of Co-Type Nitrile Hydratase Beta-H71L From Pseudomonas Putida.
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 3 of Crystal Structure of Co-Type Nitrile Hydratase Beta-H71L From Pseudomonas Putida. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
E:Co212
b:11.3
occ:1.00
|
N
|
E:CSD117
|
2.0
|
13.0
|
1.0
|
N
|
E:SER116
|
2.0
|
12.2
|
1.0
|
SG
|
E:CSD115
|
2.2
|
10.3
|
1.0
|
SG
|
E:CSD117
|
2.2
|
13.8
|
1.0
|
SG
|
E:CYS112
|
2.3
|
12.5
|
1.0
|
C
|
E:SER116
|
2.8
|
11.9
|
1.0
|
CA
|
E:SER116
|
2.9
|
10.3
|
1.0
|
OD2
|
E:CSD117
|
2.9
|
15.9
|
1.0
|
CA
|
E:CSD117
|
3.1
|
13.7
|
1.0
|
C
|
E:CSD115
|
3.1
|
13.6
|
1.0
|
CB
|
E:CSD117
|
3.1
|
13.0
|
1.0
|
OD2
|
E:CSD115
|
3.1
|
11.9
|
1.0
|
CB
|
E:CSD115
|
3.2
|
8.0
|
1.0
|
OD1
|
E:CSD115
|
3.3
|
18.8
|
1.0
|
CB
|
E:CYS112
|
3.4
|
11.6
|
1.0
|
CA
|
E:CSD115
|
3.4
|
11.8
|
1.0
|
OD1
|
E:CSD117
|
3.7
|
26.8
|
1.0
|
OG
|
E:SER116
|
3.7
|
16.2
|
1.0
|
N
|
E:CSD115
|
3.9
|
8.9
|
1.0
|
CB
|
E:SER116
|
3.9
|
9.7
|
1.0
|
O
|
E:SER116
|
4.0
|
11.7
|
1.0
|
O
|
E:CSD115
|
4.2
|
10.2
|
1.0
|
C
|
E:CSD117
|
4.3
|
11.0
|
1.0
|
O
|
E:CSD117
|
4.6
|
11.1
|
1.0
|
NH2
|
F:ARG149
|
4.8
|
14.0
|
1.0
|
CA
|
E:CYS112
|
4.8
|
10.8
|
1.0
|
C
|
E:LEU114
|
4.9
|
11.9
|
1.0
|
O
|
E:CYS112
|
4.9
|
13.5
|
1.0
|
|
Cobalt binding site 4 out
of 4 in 3qyh
Go back to
Cobalt Binding Sites List in 3qyh
Cobalt binding site 4 out
of 4 in the Crystal Structure of Co-Type Nitrile Hydratase Beta-H71L From Pseudomonas Putida.
Mono view
Stereo pair view
|
A full contact list of Cobalt with other atoms in the Co binding
site number 4 of Crystal Structure of Co-Type Nitrile Hydratase Beta-H71L From Pseudomonas Putida. within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
G:Co212
b:12.6
occ:1.00
|
N
|
G:CSD117
|
1.9
|
15.4
|
1.0
|
N
|
G:SER116
|
2.1
|
11.8
|
1.0
|
SG
|
G:CSD115
|
2.1
|
13.4
|
1.0
|
SG
|
G:CSD117
|
2.2
|
12.6
|
1.0
|
SG
|
G:CYS112
|
2.4
|
13.3
|
1.0
|
C
|
G:SER116
|
2.8
|
18.2
|
1.0
|
CA
|
G:SER116
|
2.9
|
13.9
|
1.0
|
CA
|
G:CSD117
|
3.0
|
19.1
|
1.0
|
OD2
|
G:CSD117
|
3.0
|
23.0
|
1.0
|
CB
|
G:CSD117
|
3.0
|
13.7
|
1.0
|
C
|
G:CSD115
|
3.1
|
19.0
|
1.0
|
OD2
|
G:CSD115
|
3.2
|
13.2
|
1.0
|
CB
|
G:CSD115
|
3.2
|
13.5
|
1.0
|
OD1
|
G:CSD115
|
3.2
|
18.1
|
1.0
|
CB
|
G:CYS112
|
3.4
|
11.3
|
1.0
|
CA
|
G:CSD115
|
3.4
|
15.1
|
1.0
|
OD1
|
G:CSD117
|
3.7
|
31.3
|
1.0
|
OG
|
G:SER116
|
3.8
|
17.3
|
1.0
|
N
|
G:CSD115
|
3.9
|
11.5
|
1.0
|
CB
|
G:SER116
|
3.9
|
13.8
|
1.0
|
O
|
G:SER116
|
4.0
|
13.9
|
1.0
|
O
|
G:CSD115
|
4.2
|
15.5
|
1.0
|
C
|
G:CSD117
|
4.3
|
12.4
|
1.0
|
O
|
G:CSD117
|
4.6
|
16.3
|
1.0
|
CA
|
G:CYS112
|
4.8
|
11.3
|
1.0
|
NH2
|
H:ARG149
|
4.8
|
14.3
|
1.0
|
C
|
G:LEU114
|
4.9
|
11.9
|
1.0
|
O
|
G:CYS112
|
4.9
|
13.7
|
1.0
|
|
Reference:
H.R.Brodkin,
W.R.Novak,
A.C.Milne,
J.A.D'aquino,
N.M.Karabacak,
I.G.Goldberg,
J.N.Agar,
M.S.Payne,
G.A.Petsko,
M.J.Ondrechen,
D.Ringe.
Evidence of the Participation of Remote Residues in the Catalytic Activity of Co-Type Nitrile Hydratase From Pseudomonas Putida. Biochemistry V. 50 4923 2011.
ISSN: ISSN 0006-2960
PubMed: 21473592
DOI: 10.1021/BI101761E
Page generated: Tue Jul 30 16:27:38 2024
|